B-D DRAKE WILLOCK #7000 SERIES ULTRAF

B-D DRAKE WILLOCK #7000 SERIES ULTRAF is an FDA 510(k)-cleared medical device (K811591) manufactured by Bd Becton Dickinson Vacutainer Systems Preanalytic. This device is classified under the Gastroenterology, Urology specialty. FDA Device Class II (Special Controls) — moderate risk, requires 510(k) clearance. FDA clearance granted on July 9, 1981. Regulation: 8.